Cryopreservation of the rabbit cornea: freezing with dimethyl sulphoxide in air or in medium.

There have been considerable difficulties in developing a satisfactory method for the cryopreservation of corneas. In this paper we describe the effect of two variables that appear to influence the effectiveness of preservation, the concentration of cryoprotectant and the medium that surrounds the cornea during freezing. Rabbit corneas were exposed to the cryoprotectant dimethyl sulphoxide (Me2SO) in concentrations of 1 or 2 mol/l in a high-potassium well-buffered solution, and then cooled to -196 degrees C either in air or surrounded by 5 ml of the Me2SO solution. After storage at -196 degrees C, thawing and removal of the Me2SO, survival was assessed by electron microscopy and measurement of stromal thickness during perfusion on the specular microscope. The least degree of damage was observed when corneas were equilibrated with 1M Me2SO and frozen in air. The evidence suggests that 2M may be an excessive concentration of Me2SO in this system and that damage to the stroma may be reduced by freezing the cornea in air rather than surrounded by the Me2SO solution.

[1]  M. Taylor,et al.  Cryopreservation of rabbit corneas: assessment by microscopy and transplantation. , 1985, The British journal of ophthalmology.

[2]  M. Taylor Clinical cryobiology of tissues: preservation of corneas. , 1985, Cryobiology.

[3]  M. Taylor,et al.  A new preservation solution for storage of corneas at low temperatures. , 1985, Current eye research.

[4]  P. Madden,et al.  An improved method of corneal cryopreservation , 1982 .

[5]  T. Olsen,et al.  POST‐OPERATIVE THICKNESS AND ENDOTHELIAL CELL DENSITY IN CULTIVATED, CRYOPRESERVED HUMAN CORNEAL GRAFTS , 1982, Acta ophthalmologica.

[6]  M. Taylor,et al.  Freeze‐substitution and isothermal freeze‐fixation studies to elucidate the pattern of ice formation in smooth muscle at 252 K (‐21°C) , 1982, Journal of microscopy.

[7]  Kaufman He Corneal cryopreservation and its clinical application. , 1976 .

[8]  A. Silberberg,et al.  In vitro study of the influence of some factors important for any physicochemical characterization of loose connective tissue in the microcirculation. , 1974, Microvascular research.

[9]  D. Pegg,et al.  A multirate small-volume cooling machine. , 1974, Cryobiology.

[10]  H. Edelhauser,et al.  Reversibility of ultrastructural freeze-thaw-induced injury: demonstration in the endothelium of cryopreserved corneal tissue. , 1972, Archives of ophthalmology.

[11]  D. Maurice,et al.  The metabolic basis to the fluid pump in the cornea , 1972, The Journal of physiology.

[12]  F. O. Mueller Short-term experiments on grafting fresh and frozen corneal tissue in dogs. , 1968, The British journal of ophthalmology.

[13]  T. Otori Electrolyte content of the rabbit corneal stroma. , 1967, Experimental eye research.

[14]  J. E. Robbins,et al.  Preservation of viable corneal tissue. , 1965, Cryobiology.

[15]  P. Trevor-Roper,et al.  Use of Deep-frozen Human Cornea in Full-thickness Grafts , 1964, British medical journal.

[16]  F. O. Mueller TECHNIQUES FOR FULL-THICKNESS KERATOPLASTY IN RABBITS USING FRESH AND FROZEN CORNEAL TISSUE* , 1964, The British journal of ophthalmology.

[17]  M. Ashwood‐Smith,et al.  Some in vitro studies on rabbit corneal tissue. , 1963, Experimental eye research.

[18]  V. Kinsey THE CHEMICAL COMPOSITION AND THE OSMOTIC PRESSURE OF THE AQUEOUS HUMOR AND PLASMA OF THE RABBIT , 1951, The Journal of general physiology.